Impact of genomics on research in the rat.

Abstract:

:The need to translate genes to function has positioned the rat as an invaluable animal model for genomic research. The significant increase in genomic resources in recent years has had an immediate functional application in the rat. Many of the resources for translational research are already in place and are ready to be combined with the years of physiological knowledge accumulated in numerous rat models, which is the subject of this perspective. Based on the successes to date and the research projects under way to further enhance the infrastructure of the rat, we also project where research in the rat will be in the near future. The impact of the rat genome project has just started, but it is an exciting time with tremendous progress.

journal_name

Genome Res

journal_title

Genome research

authors

Lazar J,Moreno C,Jacob HJ,Kwitek AE

doi

10.1101/gr.3744005

subject

Has Abstract

pub_date

2005-12-01 00:00:00

pages

1717-28

issue

12

eissn

1088-9051

issn

1549-5469

pii

15/12/1717

journal_volume

15

pub_type

杂志文章,评审
  • The effect of genotype and in utero environment on interindividual variation in neonate DNA methylomes.

    abstract::Integrating the genotype with epigenetic marks holds the promise of better understanding the biology that underlies the complex interactions of inherited and environmental components that define the developmental origins of a range of disorders. The quality of the in utero environment significantly influences health o...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.171439.113

    authors: Teh AL,Pan H,Chen L,Ong ML,Dogra S,Wong J,MacIsaac JL,Mah SM,McEwen LM,Saw SM,Godfrey KM,Chong YS,Kwek K,Kwoh CK,Soh SE,Chong MF,Barton S,Karnani N,Cheong CY,Buschdorf JP,Stünkel W,Kobor MS,Meaney MJ,Gluckma

    更新日期:2014-07-01 00:00:00

  • Genome dynamics in aging mice.

    abstract::Random spontaneous genome rearrangements are difficult to detect in vivo, especially in postmitotic tissues. Using a lacZ-plasmid reporter mouse model, we have previously presented evidence for the accumulation of large genome rearrangements in various tissues, including postmitotic tissues, during aging. These rearra...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.125502

    authors: Dollé ME,Vijg J

    更新日期:2002-11-01 00:00:00

  • Optical mapping of BAC clones from the human Y chromosome DAZ locus.

    abstract::The accurate mapping of clones derived from genomic regions containing complex arrangements of repeated elements presents special problems for DNA sequencers. Recent advances in the automation of optical mapping have enabled us to map a set of 16 BAC clones derived from the DAZ locus of the human Y chromosome long arm...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.112100

    authors: Giacalone J,Delobette S,Gibaja V,Ni L,Skiadas Y,Qi R,Edington J,Lai Z,Gebauer D,Zhao H,Anantharaman T,Mishra B,Brown LG,Saxena R,Page DC,Schwartz DC

    更新日期:2000-09-01 00:00:00

  • Cell-type, allelic, and genetic signatures in the human pancreatic beta cell transcriptome.

    abstract::Elucidating the pathophysiology and molecular attributes of common disorders as well as developing targeted and effective treatments hinges on the study of the relevant cell type and tissues. Pancreatic beta cells within the islets of Langerhans are centrally involved in the pathogenesis of both type 1 and type 2 diab...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.150706.112

    authors: Nica AC,Ongen H,Irminger JC,Bosco D,Berney T,Antonarakis SE,Halban PA,Dermitzakis ET

    更新日期:2013-09-01 00:00:00

  • Next-generation sequencing identifies the natural killer cell microRNA transcriptome.

    abstract::Natural killer (NK) cells are innate lymphocytes important for early host defense against infectious pathogens and surveillance against malignant transformation. Resting murine NK cells regulate the translation of effector molecule mRNAs (e.g., granzyme B, GzmB) through unclear molecular mechanisms. MicroRNAs (miRNAs)...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.107995.110

    authors: Fehniger TA,Wylie T,Germino E,Leong JW,Magrini VJ,Koul S,Keppel CR,Schneider SE,Koboldt DC,Sullivan RP,Heinz ME,Crosby SD,Nagarajan R,Ramsingh G,Link DC,Ley TJ,Mardis ER

    更新日期:2010-11-01 00:00:00

  • Prokaryotic phylogenies inferred from protein structural domains.

    abstract::The determination of the phylogenetic relationships among microorganisms has long relied primarily on gene sequence information. Given that prokaryotic organisms often lack morphological characteristics amenable to phylogenetic analysis, prokaryotic phylogenies, in particular, are often based on sequence data. In this...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.3033805

    authors: Deeds EJ,Hennessey H,Shakhnovich EI

    更新日期:2005-03-01 00:00:00

  • Allele-specific methylation is prevalent and is contributed by CpG-SNPs in the human genome.

    abstract::In diploid mammalian genomes, parental alleles can exhibit different methylation patterns (allele-specific DNA methylation, ASM), which have been documented in a small number of cases except for the imprinted regions and X chromosomes in females. We carried out a chromosome-wide survey of ASM across 16 human pluripote...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.104695.109

    authors: Shoemaker R,Deng J,Wang W,Zhang K

    更新日期:2010-07-01 00:00:00

  • HERC2 rs12913832 modulates human pigmentation by attenuating chromatin-loop formation between a long-range enhancer and the OCA2 promoter.

    abstract::Pigmentation of skin, eye, and hair reflects some of the most evident common phenotypes in humans. Several candidate genes for human pigmentation are identified. The SNP rs12913832 has strong statistical association with human pigmentation. It is located within an intron of the nonpigment gene HERC2, 21 kb upstream of...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.128652.111

    authors: Visser M,Kayser M,Palstra RJ

    更新日期:2012-03-01 00:00:00

  • A burst of protein sequence evolution and a prolonged period of asymmetric evolution follow gene duplication in yeast.

    abstract::It is widely accepted that newly arisen duplicate gene pairs experience an altered selective regime that is often manifested as an increase in the rate of protein sequence evolution. Many details about the nature of the rate acceleration remain unknown, however, including its typical magnitude and duration, and whethe...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6341207

    authors: Scannell DR,Wolfe KH

    更新日期:2008-01-01 00:00:00

  • Spidey: a tool for mRNA-to-genomic alignments.

    abstract::We have developed a computer program that aligns spliced sequences to genomic sequences, using local alignment algorithms and heuristics to put together a global spliced alignment. Spidey can produce reliable alignments quickly, even when confronted with noise from alternative splicing, polymorphisms, sequencing error...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.195301

    authors: Wheelan SJ,Church DM,Ostell JM

    更新日期:2001-11-01 00:00:00

  • Genomics and hearing impairment.

    abstract::Hearing impairment is clinically and genetically heterogeneous. There are >400 disorders in which hearing impairment is a characteristic of the syndrome, and family studies demonstrate that there are at least 30 autosomal loci for nonsyndromic hearing impairment. The genes that have been identified encode diaphanous (...

    journal_title:Genome research

    pub_type: 历史文章,杂志文章,评审

    doi:

    authors: Keats BJ,Berlin CI

    更新日期:1999-01-01 00:00:00

  • How does replication-associated mutational pressure influence amino acid composition of proteins?

    abstract::We have performed detrended DNA walks on whole prokaryotic genomes, on noncoding sequences and, separately, on each position in codons of coding sequences. Our method enables us to distinguish between the mutational pressure associated with replication and the mutational pressure associated with transcription and othe...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:

    authors: MackiewiczP,Gierlik A,Kowalczuk M,Dudek MR,Cebrat S

    更新日期:1999-05-01 00:00:00

  • Why do human diversity levels vary at a megabase scale?

    abstract::Levels of diversity vary across the human genome. This variation is caused by two forces: differences in mutation rates and the differential impact of natural selection. Pertinent to the question of the relative importance of these two forces is the observation that both diversity within species and interspecies diver...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.3461105

    authors: Hellmann I,Prüfer K,Ji H,Zody MC,Pääbo S,Ptak SE

    更新日期:2005-09-01 00:00:00

  • RNA expression profiling at the single molecule level.

    abstract::We developed a microarray platform for PCR amplification-independent expression profiling of minute samples. A novel scanning system combined with specialized biochips enables detection down to individual fluorescent oligonucleotide molecules specifically hybridized to their complementary sequence over the entire bioc...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.4999906

    authors: Hesse J,Jacak J,Kasper M,Regl G,Eichberger T,Winklmayr M,Aberger F,Sonnleitner M,Schlapak R,Howorka S,Muresan L,Frischauf AM,Schütz GJ

    更新日期:2006-08-01 00:00:00

  • Inference of population genetic parameters in metagenomics: a clean look at messy data.

    abstract::Metagenomic projects generate short, overlapping fragments of DNA sequence, each deriving from a different individual. We report a new method for inferring the scaled mutation rate, theta = 2Neu, and the scaled exponential growth rate, R = Ner, from the site-frequency spectrum of these data while accounting for sequen...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5431206

    authors: Johnson PL,Slatkin M

    更新日期:2006-10-01 00:00:00

  • Comparative genomics of the Archaea (Euryarchaeota): evolution of conserved protein families, the stable core, and the variable shell.

    abstract::Comparative analysis of the protein sequences encoded in the four euryarchaeal species whose genomes have been sequenced completely (Methanococcus jannaschii, Methanobacterium thermoautotrophicum, Archaeoglobus fulgidus, and Pyrococcus horikoshii) revealed 1326 orthologous sets, of which 543 are represented in all fou...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:

    authors: Makarova KS,Aravind L,Galperin MY,Grishin NV,Tatusov RL,Wolf YI,Koonin EV

    更新日期:1999-07-01 00:00:00

  • YY1 and CTCF orchestrate a 3D chromatin looping switch during early neural lineage commitment.

    abstract::CTCF is an architectural protein with a critical role in connecting higher-order chromatin folding in pluripotent stem cells. Recent reports have suggested that CTCF binding is more dynamic during development than previously appreciated. Here, we set out to understand the extent to which shifts in genome-wide CTCF occ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.215160.116

    authors: Beagan JA,Duong MT,Titus KR,Zhou L,Cao Z,Ma J,Lachanski CV,Gillis DR,Phillips-Cremins JE

    更新日期:2017-07-01 00:00:00

  • A general approach for identifying distant regulatory elements applied to the Gdf6 gene.

    abstract::Regulatory sequences in higher genomes can map large distances from gene coding regions, and cannot yet be identified by simple inspection of primary DNA sequence information. Here we describe an efficient method of surveying large genomic regions for gene regulatory information, and subdividing complex sets of distan...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.1306003

    authors: Mortlock DP,Guenther C,Kingsley DM

    更新日期:2003-09-01 00:00:00

  • Comparing genomes within the species Mycobacterium tuberculosis.

    abstract::The study of genetic variability within natural populations of pathogens may provide insight into their evolution and pathogenesis. We used a Mycobacterium tuberculosis high-density oligonucleotide microarray to detect small-scale genomic deletions among 19 clinically and epidemiologically well-characterized isolates ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.166401

    authors: Kato-Maeda M,Rhee JT,Gingeras TR,Salamon H,Drenkow J,Smittipat N,Small PM

    更新日期:2001-04-01 00:00:00

  • Dissecting transcription regulatory pathways through a new bacterial one-hybrid reporter system.

    abstract::Sequence-specific DNA-binding transcription factors have widespread biological significance in the regulation of gene expression. However, in lower prokaryotes and eukaryotic metazoans, it is usually difficult to find transcription regulatory factors that recognize specific target promoters. To address this, we have d...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.086595.108

    authors: Guo M,Feng H,Zhang J,Wang W,Wang Y,Li Y,Gao C,Chen H,Feng Y,He ZG

    更新日期:2009-07-01 00:00:00

  • Genomic localization of RNA binding proteins reveals links between pre-mRNA processing and transcription.

    abstract::Pre-mRNA processing often occurs in coordination with transcription thereby coupling these two key regulatory events. As such, many proteins involved in mRNA processing associate with the transcriptional machinery and are in proximity to DNA. This proximity allows for the mapping of the genomic associations of RNA bin...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5211806

    authors: Swinburne IA,Meyer CA,Liu XS,Silver PA,Brodsky AS

    更新日期:2006-07-01 00:00:00

  • Ride the wavelet: A multiscale analysis of genomic contexts flanking small insertions and deletions.

    abstract::Recent studies have revealed that insertions and deletions (indels) are more different in their formation than previously assumed. What remains enigmatic is how the local DNA sequence context contributes to these differences. To investigate the relative impact of various molecular mechanisms to indel formation, we ana...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.088922.108

    authors: Kvikstad EM,Chiaromonte F,Makova KD

    更新日期:2009-07-01 00:00:00

  • The human phosphotyrosine signaling network: evolution and hotspots of hijacking in cancer.

    abstract::Phosphotyrosine (pTyr) signaling, which plays a central role in cell-cell and cell-environment interactions, has been considered to be an evolutionary innovation in multicellular metazoans. However, neither the emergence nor the evolution of the human pTyr signaling system is currently understood. Tyrosine kinase (TK)...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.128819.111

    authors: Li L,Tibiche C,Fu C,Kaneko T,Moran MF,Schiller MR,Li SS,Wang E

    更新日期:2012-07-01 00:00:00

  • High-throughput plasmid purification for capillary sequencing.

    abstract::The need for expeditious and inexpensive methods for high-throughput DNA sequencing has been highlighted by the accelerated pace of genome DNA sequencing over the past year. At the Joint Genome Institute, the throughput in terms of high-quality bases per day has increased over 20-fold during the past 18 mo, reaching a...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.167801

    authors: Elkin CJ,Richardson PM,Fourcade HM,Hammon NM,Pollard MJ,Predki PF,Glavina T,Hawkins TL

    更新日期:2001-07-01 00:00:00

  • Genomic organization of the sex-determining and adjacent regions of the sex chromosomes of medaka.

    abstract::Sequencing of the human Y chromosome has uncovered the peculiarities of the genomic organization of a heterogametic sex chromosome of old evolutionary age, and has led to many insights into the evolutionary changes that occurred during its long history. We have studied the genomic organization of the medaka fish Y chr...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5016106

    authors: Kondo M,Hornung U,Nanda I,Imai S,Sasaki T,Shimizu A,Asakawa S,Hori H,Schmid M,Shimizu N,Schartl M

    更新日期:2006-07-01 00:00:00

  • The human homolog T of the mouse T(Brachyury) gene; gene structure, cDNA sequence, and assignment to chromosome 6q27.

    abstract::We have cloned the human gene encoding the transcription factor T. T protein is vital for the formation of posterior mesoderm and axial development in all vertebrates. Brachyury mutant mice, which lack T protein, die in utero with abnormal notochord, posterior somites, and allantois. We have identified human T genomic...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6.3.226

    authors: Edwards YH,Putt W,Lekoape KM,Stott D,Fox M,Hopkinson DA,Sowden J

    更新日期:1996-03-01 00:00:00

  • Dynamic effects of interacting genes underlying rice flowering-time phenotypic plasticity and global adaptation.

    abstract::The phenotypic variation of living organisms is shaped by genetics, environment, and their interaction. Understanding phenotypic plasticity under natural conditions is hindered by the apparently complex environment and the interacting genes and pathways. Herein, we report findings from the dissection of rice flowering...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.255703.119

    authors: Guo T,Mu Q,Wang J,Vanous AE,Onogi A,Iwata H,Li X,Yu J

    更新日期:2020-05-01 00:00:00

  • Transcriptional alterations in glioma result primarily from DNA methylation-independent mechanisms.

    abstract::In cancer cells, aberrant DNA methylation is commonly associated with transcriptional alterations, including silencing of tumor suppressor genes. However, multiple epigenetic mechanisms, including polycomb repressive marks, contribute to gene deregulation in cancer. To dissect the relative contribution of DNA methylat...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.249219.119

    authors: Court F,Le Boiteux E,Fogli A,Müller-Barthélémy M,Vaurs-Barrière C,Chautard E,Pereira B,Biau J,Kemeny JL,Khalil T,Karayan-Tapon L,Verrelle P,Arnaud P

    更新日期:2019-10-01 00:00:00

  • A computational genomics approach to identify cis-regulatory modules from chromatin immunoprecipitation microarray data--a case study using E2F1.

    abstract::Advances in high-throughput technologies, such as ChIP-chip, and the completion of human and mouse genomic sequences now allow analysis of the mechanisms of gene regulation on a systems level. In this study, we have developed a computational genomics approach (termed ChIPModules), which begins with experimentally dete...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5520206

    authors: Jin VX,Rabinovich A,Squazzo SL,Green R,Farnham PJ

    更新日期:2006-12-01 00:00:00

  • A highly efficient procedure for site-specific mutagenesis of full-length plasmids using Vent DNA polymerase.

    abstract::Careful titration of Vent polymerase activity allows efficient amplification of full-length plasmids (12 kb). The high processivity and fidelity of this enzyme made oligonucleotide-directed site-specific mutagenesis of plasmids a straight-forward process. Using only two primers, a mutagenic and a complementary, single...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5.4.404

    authors: Byrappa S,Gavin DK,Gupta KC

    更新日期:1995-11-01 00:00:00